Clin2
NCT05054465Possibly a fitNot yet recruiting

Venetoclax and navitoclax after transplant for high-risk T-ALL

Acute Lymphoblastic Leukemia

Treatments studied

Part of Blood & lymphatic, Cancer, Immune system & allergy clinical trials.

This trial tests whether adding venetoclax and navitoclax around the time of an allogeneic stem cell transplant can help prevent relapse in people with high-risk T-ALL (or related T-cell blood cancers). It also looks at whether these medicines can be used after transplant to help keep the disease under control.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
48 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Be at least 18 years old when you sign the consent.
  • Have a new diagnosis of T-ALL, T-LBL, or MPAL T/myeloid (according to WHO 2016).
  • Be in your first complete response and your doctors plan an allogeneic stem cell transplant (alloSCT).
  • Your initial cancer treatment must include a BFM-style induction with asparaginase (not a different induction style like HyperCVAD).
  • Your blood and organ tests must be strong enough: platelets and neutrophils at set minimums, liver enzymes/bilirubin not too high, and kidney function (creatinine clearance) at least 30 mL/min.
  • You must be able to use effective birth control and agree to pregnancy testing if you can become pregnant, and you must not be pregnant or breastfeeding.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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